Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/- | Ancestral: A
Location

Chromosome 4:74902528 (forward strand) | View in location tab

Co-located

with dbSNP rs199517714 (A/T)

Most severe consequence

This variation has 2 HGVS names - click the plus to show

Variation displays